Cargando…
Existence of Circulating Mitochondria in Human and Animal Peripheral Blood
Mitochondria are usually located in the cytoplasm of cells where they generate adenosine triphosphate (ATP) to empower cellular functions. However, we found circulating mitochondria in human and animal blood. Electron microscopy confirmed the presence of mitochondria in adult human blood plasma. Flo...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139699/ https://www.ncbi.nlm.nih.gov/pubmed/32204530 http://dx.doi.org/10.3390/ijms21062122 |
_version_ | 1783518826376200192 |
---|---|
author | Song, Xiang Hu, Wei Yu, Haibo Wang, Honglan Zhao, Yelu Korngold, Robert Zhao, Yong |
author_facet | Song, Xiang Hu, Wei Yu, Haibo Wang, Honglan Zhao, Yelu Korngold, Robert Zhao, Yong |
author_sort | Song, Xiang |
collection | PubMed |
description | Mitochondria are usually located in the cytoplasm of cells where they generate adenosine triphosphate (ATP) to empower cellular functions. However, we found circulating mitochondria in human and animal blood. Electron microscopy confirmed the presence of mitochondria in adult human blood plasma. Flow cytometry analyses demonstrated that circulating mitochondria from the plasma of human cord blood and adult peripheral blood displayed the immune tolerance-associated membrane molecules such as CD270 and PD-L1 (programmed cell death-ligand 1). Similar data were obtained from fetal bovine serum (FBS) and horse serum of different vendors. Mitochondria remained detectable even after 56 °C heat inactivation. A real-time PCR array revealed purified mitochondria from animal sera expressed several genes that contribute to human T- and B-cell activation. Transwell experiments confirmed the migration capability of mitochondria through their expression of the chemokine receptor CXCR4 in responses to its ligand stromal-derived factor-1α (SDF-1α). Functional analysis established that human plasma mitochondria stimulated the proliferation of anti-CD3/CD28 bead-activated PBMC, up-regulated the percentage of activated CD4(+) T and CD8(+) T cells, and reduced the production of inflammatory cytokines. These findings suggested that the existence of circulating mitochondria in blood may function as a novel mediator for cell-cell communications and maintenance of homeostasis. Plasma-related products should be cautiously utilized in cell cultures due to the mitochondrial contamination. |
format | Online Article Text |
id | pubmed-7139699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71396992020-04-10 Existence of Circulating Mitochondria in Human and Animal Peripheral Blood Song, Xiang Hu, Wei Yu, Haibo Wang, Honglan Zhao, Yelu Korngold, Robert Zhao, Yong Int J Mol Sci Article Mitochondria are usually located in the cytoplasm of cells where they generate adenosine triphosphate (ATP) to empower cellular functions. However, we found circulating mitochondria in human and animal blood. Electron microscopy confirmed the presence of mitochondria in adult human blood plasma. Flow cytometry analyses demonstrated that circulating mitochondria from the plasma of human cord blood and adult peripheral blood displayed the immune tolerance-associated membrane molecules such as CD270 and PD-L1 (programmed cell death-ligand 1). Similar data were obtained from fetal bovine serum (FBS) and horse serum of different vendors. Mitochondria remained detectable even after 56 °C heat inactivation. A real-time PCR array revealed purified mitochondria from animal sera expressed several genes that contribute to human T- and B-cell activation. Transwell experiments confirmed the migration capability of mitochondria through their expression of the chemokine receptor CXCR4 in responses to its ligand stromal-derived factor-1α (SDF-1α). Functional analysis established that human plasma mitochondria stimulated the proliferation of anti-CD3/CD28 bead-activated PBMC, up-regulated the percentage of activated CD4(+) T and CD8(+) T cells, and reduced the production of inflammatory cytokines. These findings suggested that the existence of circulating mitochondria in blood may function as a novel mediator for cell-cell communications and maintenance of homeostasis. Plasma-related products should be cautiously utilized in cell cultures due to the mitochondrial contamination. MDPI 2020-03-19 /pmc/articles/PMC7139699/ /pubmed/32204530 http://dx.doi.org/10.3390/ijms21062122 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Song, Xiang Hu, Wei Yu, Haibo Wang, Honglan Zhao, Yelu Korngold, Robert Zhao, Yong Existence of Circulating Mitochondria in Human and Animal Peripheral Blood |
title | Existence of Circulating Mitochondria in Human and Animal Peripheral Blood |
title_full | Existence of Circulating Mitochondria in Human and Animal Peripheral Blood |
title_fullStr | Existence of Circulating Mitochondria in Human and Animal Peripheral Blood |
title_full_unstemmed | Existence of Circulating Mitochondria in Human and Animal Peripheral Blood |
title_short | Existence of Circulating Mitochondria in Human and Animal Peripheral Blood |
title_sort | existence of circulating mitochondria in human and animal peripheral blood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139699/ https://www.ncbi.nlm.nih.gov/pubmed/32204530 http://dx.doi.org/10.3390/ijms21062122 |
work_keys_str_mv | AT songxiang existenceofcirculatingmitochondriainhumanandanimalperipheralblood AT huwei existenceofcirculatingmitochondriainhumanandanimalperipheralblood AT yuhaibo existenceofcirculatingmitochondriainhumanandanimalperipheralblood AT wanghonglan existenceofcirculatingmitochondriainhumanandanimalperipheralblood AT zhaoyelu existenceofcirculatingmitochondriainhumanandanimalperipheralblood AT korngoldrobert existenceofcirculatingmitochondriainhumanandanimalperipheralblood AT zhaoyong existenceofcirculatingmitochondriainhumanandanimalperipheralblood |